Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Dermatology Department, Hospital Clínic, Institut d'Investigacions Biomediques August Pi i Sunyer, Universitat de Barcelona, and CIBER de Enfermedades Raras, Instituto de Salud Carlos III, Barcelona, Spain.
Dermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Dermatology, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
J Am Acad Dermatol. 2019 Jun;80(6):1585-1593. doi: 10.1016/j.jaad.2018.09.014. Epub 2018 Sep 20.
Multiple BRCA1-associated protein 1 (BAP1)-inactivated melanocytic tumors (BIMTs) have been associated with a familial cancer syndrome involving germline mutations in BAP1.
We sought to describe the clinical and dermoscopic features of BIMTs.
This was a retrospective, multicenter, case-control study. Participating centers contributed clinical data, dermoscopic images, and histopathologic data of biopsy-proven BIMTs. We compared the dermoscopic features between BIMTs and control patients.
The dataset consisted of 48 BIMTs from 31 patients (22 women; median age 37 years) and 80 control patients. Eleven patients had a BAP1 germline mutation. Clinically, most BIMTs presented as pink, dome-shaped papules (n = 24). Dermoscopically, we identified 5 patterns: structureless pink-to-tan with irregular eccentric dots/globules (n = 14, 29.8%); structureless pink-to-tan with peripheral vessels (n = 10, 21.3%); structureless pink-to-tan (n = 7, 14.9%); a network with raised, structureless, pink-to-tan areas (n = 7, 14.9%); and globular pattern (n = 4, 8.5%). The structureless with eccentric dots/globules pattern and network with raised structureless areas pattern were only identified in BIMT and were more common in patients with BAP1 germline mutations (P < .0001 and P = .001, respectively).
Limitations included our small sample size, retrospective design, the absence of germline genetic testing in all patients, and inclusion bias toward more atypical-looking BIMTs.
Dome-shaped papules with pink-to-tan structureless areas and peripheral irregular dots/globules or network should raise the clinical suspicion for BIMT.
多个 BRCA1 相关蛋白 1(BAP1)失活的黑色素细胞肿瘤(BIMTs)与涉及 BAP1 种系突变的家族性癌症综合征有关。
我们旨在描述 BIMTs 的临床和皮肤镜特征。
这是一项回顾性、多中心、病例对照研究。参与中心提供了经活检证实的 BIMTs 的临床数据、皮肤镜图像和组织病理学数据。我们比较了 BIMTs 与对照组患者的皮肤镜特征。
数据集包括 31 名患者(22 名女性;中位年龄 37 岁)的 48 个 BIMTs 和 80 名对照患者。11 名患者存在 BAP1 种系突变。临床上,大多数 BIMTs 表现为粉红色、圆顶状丘疹(n=24)。皮肤镜下,我们发现了 5 种模式:无结构的粉红色至棕褐色,具有不规则偏心点/球(n=14,29.8%);无结构的粉红色至棕褐色,伴周边血管(n=10,21.3%);无结构的粉红色至棕褐色(n=7,14.9%);一个带有隆起的无结构粉红色至棕褐色区域的网络(n=7,14.9%);和球形模式(n=4,8.5%)。无结构伴偏心点/球模式和带有隆起的无结构区域的网络模式仅在 BIMT 中被识别,并且在存在 BAP1 种系突变的患者中更为常见(P<0.0001 和 P=0.001)。
我们的样本量小、回顾性设计、并非所有患者都进行了种系基因检测以及存在对更具非典型外观的 BIMTs 的纳入偏倚等限制因素。
具有粉红色至棕褐色无结构区域和周边不规则点/球或网络的圆顶状丘疹应引起对 BIMT 的临床怀疑。